Primary Device ID | 00810050861960 |
NIH Device Record Key | 3ca7be45-d7df-448b-9d40-c3b31cbcdc23 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ServiPlex |
Version Model Number | 0404-0301-01-01 |
Company DUNS | 556196210 |
Company Name | LIFEPORT, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com | |
Phone | 360-225-1212 |
CustomerService@lifeport.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810050861960 [Primary] |
FOX | Stand, Infusion |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-06 |
Device Publish Date | 2022-04-28 |
00810050861977 | ASSEMBLY - SYSTEMS – SERVIPLEX |
00810050861960 | ASSEMBLY - SYSTEMS – SERVIPLEX |
00810050862905 | ASSEMBLY - SERVIPLEX |
00810050862912 | ASSEMBLY - SERVIPLEX |